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Identification of invasive whitefly Bemisia tabaci cryptic species is best achieved by an integrated approach combining mating and genomic studies including complete mitochondrial DNA genomes (mitogenomes) characterization. We present the draft mitogenome of a 1920 historical B. tabaci specimen obtained using High Throughput Sequencing (HTS) technology. Our B. tabaci partial mtCOI gene best matched the B. tabaci ‘NW’ (New World) cryptic species (e.g. to AY057133; nucleotide identity: 99.85%). It has a circular genome of ca. 15,325bp with 13 protein-coding genes (PCGs), 22 tRNA’s, and two rRNA genes. A total of 43 amino acid residues differed between a Sanger-sequenced ‘NW’ mitogenome (AY521259.2) and this HTS-generated ‘NW’ mitogenome. High intra-specific amino acid conservation was observed across the partial 657 bp mitochondrial DNA COI (mtCOI) gene region used in species identification (i.e. from nucleotides 782 to 1438) when compared between both ‘NW’ (MK386668, AY521259.2) species.

The Bemisia tabaci species complex is one of the most important pests of open field and protected cropping globally. Within this complex, one species (Middle East Asia Minor 1, B. tabaci MEAM1, formerly biotype B) has been especially problematic, invading widely and spreading a large variety of plant pathogens, and developing broad spectrum pesticide resistance. Here, we fit a CLIMEX model to the distribution records of B. tabaci MEAM1, using experimental observations to calibrate its temperature responses. In fitting the model, we consider the effects of irrigation and glasshouses in extending its potential range. The validated niche model estimates its potential distribution as being considerably broader than its present known distribution, especially in the Americas, Africa and Asia. The potential distribution of the fitted model encompasses the known distribution of B. tabaci sensu lato, highlighting the magnitude of the threat posed globally by this invasive pest species complex and the viruses it vectors to open field and protected agriculture. [ABSTRACT FROM AUTHOR]

Organisms differ greatly in dispersal ability, and landscapes differ in amenability to an organism's movement. Thus, landscape structure and heterogeneity can affect genetic composition of populations. While many agricultural pests are known for their ability to disperse rapidly, it is unclear how fast and over what spatial scale insect pests might respond to the temporally dynamic agricultural landscapes they inhabit. We used population genetic analyses of a severe crop pest, a member of the Bemisia tabaci (Hemiptera: Sternorrhyncha: Aleyrodoidea: Aleyrodidea) cryptic species complex known as Middle East-Asia Minor 1 (commonly known as biotype B), to estimate spatial and temporal genetic diversity over four months of the 2006–2007 summer growing season. We examined 559 individuals from eight sites, which were scored for eight microsatellite loci. Temporal genetic structure greatly exceeded spatial structure. There was significant temporal change in local genetic composition from the beginning to the end of the season accompanied by heterozygote deficits and inbreeding. This temporal structure suggests entire cohorts of pests can occupy a large and variable agricultural landscape but are rapidly replaced. These rapid genetic fluctuations reinforce the concept that agricultural landscapes are dynamic mosaics in time and space and may contribute to better decisions for pest and insecticide resistance management. [ABSTRACT FROM AUTHOR]

The whitefly Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) is a cryptic species complex that contains some of the most damaging pests in tropical and subtropical regions. Recent studies suggested that this complex is composed of at least 24 distinct species. We use the approach from these studies to consider the identity of B. tabaci in Argentina. Previous studies have suggested the presence of a B. tabaci presumably indigenous to the Americas and referred to as the BR biotype in Argentina. We placed the entity referred to as the BR biotype within the B. tabaci cryptic species complex using whiteflies collected in soybean and bean crops in northern and central Argentina. The whiteflies were assigned using the mitochondrial cytochrome oxidase (mtCOI) gene. Four unknown haplotypes plus two Argentina sequences from GenBank formed a cluster that was basal to the rest of the New World sequences. These sequences diverged from the consensus sequence across the range of 3.6 to 4.3%. Applying the species assignment rules of recent studies suggests that the individuals from Argentina form a separate species. A fifth unknown haplotype fell within the New World putative species and formed a distinct cluster with haplotypes from Panama. These results suggest that Argentina has two indigenous species belonging to the B. tabaci cryptic species complex. Rather than using mtCOI sequencing for all B. tabaci collected, a simple random amplified polymorphic DN polymerase chain reaction diagnostic was used and tested along with previously published primers designed to work specifically with the BR biotype from Brazil. These primers were either unable to distinguish between the two indigenous members of the complex in Argentina or indicated a difference when none was evident on the basis of mtCOI sequence comparison. [ABSTRACT FROM AUTHOR]

Identifying species boundaries within morphologically indistinguishable cryptic species complexes is often contentious. For the whitefly Bemisia tabaci (Gennadius) (Hemiptera: Sternorrhyncha: Aleyrodoidea: Aleyrodidae), the lack of a clear understanding about the genetic limits of the numerous genetic groups and biotypes so far identified has resulted in a lack of consistency in the application of the terms, the approaches used to apply them and in our understanding of what genetic structure within B. tabaci means. Our response has been to use mitochondrial gene cytochrome oxidase one to consider how to clearly and consistently define genetic separation. Using Bayesian phylogenetic analysis and analysis of sequence pairwise divergence we found a considerably higher number of genetic groups than had been previously determined with two breaks in the distribution, one at 11% and another at 3.5%. At >11% divergence, 11 distinct groups were resolved, whereas at >3.5% divergence 24 groups were identified. Consensus sequences for each of these groups were determined and were shown to be useful in the correct assignment of sequences of unknown origin. The 3.5% divergence bound is consistent with species level separations in other insect taxa and suggests that B. tabaci is a cryptic species composed of at least 24 distinct species. We further show that the placement of Bemesia atriplex (Froggatt) within the B. tabaci in group adds further weight to the argument for species level separation within B. tabaci. This new analysis, which constructs consensus sequences and uses these as a standard against which unknown sequences can be compared, provides for the first time a consistent means of identifying the genetic bounds of each species with a high degree of certainty. [ABSTRACT FROM AUTHOR]

Bemisia tabaci (Hemiptera: Aleyrodidae) is a haplo-diploid species with a global distribution demonstrating strong geographical structure with eight recognizable genetic groups. Fifteen microsatellite loci (335 alleles, 6-44 alleles per locus) were derived from four of the eight groups and were then screened across 33 populations. These loci clearly differentiate the populations. The microsatellites amplified best in individuals from genetic groups rep-resenting the Mediterranean, Middle East, Asia (three groups) and Australasia/Oceania and amplified less well with populations from sub-Saharan Africa and the New World. This differential amplification pattern is a direct result of the relatedness to the microsatellite source material. [ABSTRACT FROM AUTHOR]

Identification of invasive whitefly Bemisia tabaci cryptic species is best achieved by an integrated approach combining mating and genomic studies including complete mitochondrial DNA genomes (mitogenomes) characterization. We present the draft mitogenome of a 1920 historical B. tabaci specimen obtained using High Throughput Sequencing (HTS) technology. Our B. tabaci partial mtCOI gene best matched the B. tabaci 'NW' (New World) cryptic species (e.g. to AY057133; nucleotide identity: 99.85%). It has a circular genome of ca. 15,325bp with 13 protein-coding genes (PCGs), 22 tRNA's, and two rRNA genes. A total of 43 amino acid residues differed between a Sanger-sequenced 'NW' mitogenome (AY521259.2) and this HTS-generated 'NW' mitogenome. High intra-specific amino acid conservation was observed across the partial 657 bp mitochondrial DNA COI (mtCOI) gene region used in species identification (i.e. from nucleotides 782 to 1438) when compared between both 'NW' (MK386668, AY521259.2) species. [ABSTRACT FROM AUTHOR]

The complete length of theAsia Imember of theBemisia tabacispecies complex mitochondrial DNA genome (mitogenome) is 15,210 bp (GenBank accession no. KJ778614) with an A-T biased nucleotide composition (A: 32.7%; T: 42.4%; G: 14.0%; C: 10.8%). The mitogenome consists of 13 protein-coding genes (PCGs), 22 transfer RNAs (tRNAs), 2 ribosomal RNA (rRNAs) and a 467 bp putative control region which also includes the A+T rich repeat region. All PCGs have an ATA (n = 8) or ATG (n = 5) start codon. Gene synteny ofAsia Iis overall similar toB. aferand two other members of theB. tabacispecies complexMediterraneanandNew World 1, and contains thetRNA-Ser2 located between theCytbandND1genes found inMediterraneanandNew World 1, but which is absent inB. afer. The orientation of thetRNA-Arg inAsia Iis on the “plus” strand and differed fromMediterraneanwhich is found on the “minus” strand. TheAsia Imitogenome size is currently ranked the second smallest afterB. afer(14,968 bp) followed byNew World 1(15,322 bp) andMediterranean(15,632 bp). [ABSTRACT FROM AUTHOR]